Linked Data
MyVariant Identifiers:
chr1:g.149899646A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927754A>T , CM000663.2:g.149927754A>T | GRCh38 |
| NC_000001.10:g.149899646A>T , CM000663.1:g.149899646A>T | GRCh37 |
| NC_000001.9:g.148166270A>T | NCBI36 |
| NG_032777.1:g.5499T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.9:c.6T>A MANE Select | ENSP00000271628.8:p.Ala2= | |
| ENST00000271628.8:c.6T>A | ENSP00000271628.8:p.Ala2= | |
| NM_005850.4:c.6T>A | NP_005841.1:p.Ala2= | |
| NM_005850.5:c.6T>A MANE Select | NP_005841.1:p.Ala2= |